"Molecular Genetics, Labor Dr. Heidrich & Kollegen MVZ GmbH"[submitter - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2570615	NM_001267550.2(TTN):c.71113C>G (p.Pro23705Ala)	TTN, TTN-AS1 (P14765A +5 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2578414	NM_001267550.2(TTN):c.64457T>A (p.Ile21486Asn)	TTN, TTN-AS1 (I12421N +5 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2570613	NM_001267550.2(TTN):c.50148T>G (p.Thr16716=)	TTN, TTN-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2570617	NM_001267550.2(TTN):c.44005G>A (p.Asp14669Asn)	TTN (D13028N +5 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2570614	NM_001267550.2(TTN):c.29964G>T (p.Glu9988Asp)	TTN (E9988D +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2578411	NM_133379.5(TTN):c.13560T>C (p.Asn4520=)	TTN	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2501666	NM_133379.5(TTN):c.12934C>T (p.Leu4312Phe)	TTN (L4312F)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2578413	NM_001267550.2(TTN):c.2536T>G (p.Leu846Val)	TTN (L800V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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